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Fc receptor

  An Fc receptor is a protein found on the surface of certain cells; including natural killer cells, macrophages, neutrophils and mast cells; that contribute to the protective functions of the immune system. Its name is derived from its binding specificity for a part of an antibody known as the Fc (Fragment, crystallizable) region. Fc receptors bind to antibodies that are attached to infected cells or invading pathogens. Their activity stimulates phagocytic or cytotoxic cells to destroy microbes, or infected cells by antibody-mediated phagocytosis or antibody-dependent cell-mediated cytotoxicity. Some viruses such as flaviviruses use Fc receptors to help them infect cells, by a mechanism known as antibody-dependent enhancement of infection.[1]


Classes of Fc receptor

There are several different types of Fc receptor, which are classified based on the type of antibody that they recognize; those that bind the most common class of antibody, IgG, are called Fc-gamma receptors (FcγR), those that bind IgA are called Fc-alpha receptors (FcαR) and those that bind IgE are called Fc-epsilon receptors (FcεR).

Fc-gamma receptors

All FcγRs belong to the immunoglobulin superfamily and are the most important Fc receptors for inducing phagocytosis of opsonized (coated) microbes.[2] This family includes several members; FcγRI (CD64), FcγRIIA (CD32), FcγRIIB (CD32), FcγRIIIA (CD16a), FcγRIIIB (CD16b); that differ in their antibody affinities and their molecular structure.[3] For instance, FcγRI binds to IgG more strongly than FcγRII and FcγRIII, and has an extracellular portion composed of three immunoglobulin (Ig)-like domains, one more domain than FcγRII and FcγRIII. These properties allow activation of FcγRI by a sole IgG molecule (or monomer), while the latter two Fcγ receptors must bind multiple IgG molecules within an immune complex to be activated.[2]

Another FcR is expressed on multiple cell types and is similar in structure to MHC class I. This receptor also binds IgG and is involved in preservation of this antibody.[4] However, since this Fc receptor is also involved in transferring IgG from a mother either via the placenta to her fetus or in milk to her suckling infant, it is called the neonatal Fc receptor (FcRn).[5][6] Recently this receptor has been implicated in being involved in homeostasis of IgG serum levels.

Fc-alpha receptors

Only one Fc receptor belongs to the FcαR subgroup, which is called FcαRI (or CD89).[7] FcαRI is found on the surface of neutrophils, eosinophils, monocytes, some macrophages (including Kupffer cells), and some dendritic cells.[7] It is composed of two extracellular Ig-like domains, and is a member of both the immunoglobulin superfamily and the multi-chain immune recognition receptor (MIRR) family.[2] It signals by associating with two FcRγ signaling chains.[7] Another receptor can also bind IgA, although it has higher affinity for another antibody called IgM.[8] This receptor is called the Fc-alpha/mu receptor (Fcα/μR) and is a type I transmembrane protein. With one Ig-like domain in its extracellular portion, this Fc receptor is also a member of the immunoglobulin superfamily.[9]

Fc-epsilon receptors

Two types of FcεR are known:[2]

  • the high-affinity receptor FcεRI is a member of the immunoglobulin superfamily (it has two Ig-like domains). FcεRI is found on epidermal Langerhans cells, eosinophils, mast cells and basophils.[10][11] As a result of its cellular distribution, this receptor plays a major role in controlling allergic responses. FcεRI is also expressed on antigen presenting cells, and controls the production of important immune mediators called cytokines that promote inflammation.[12]
  • the low-affinity receptor FcεRII (CD23) is a C-type lectin. FcεRII has multiple functions as a membrane-bound or soluble receptor; it controls B cell growth and differentiation and blocks IgE-binding of eosinophils, monocytes and basophils.[13]

Summary table

Receptor namePrincipal antibody ligandAffinity for ligandCell distributionEffect following binding to antibody
FcγRI (CD64) IgG1 and IgG3 High (Kd ~ 10-9 M) Macrophages
Dendritic cells
Cell activation
Activation of respiratory burst
Induction of microbe killing
FcγRIIA (CD32) IgG Low (Kd > 10-7 M) Macrophages
Langerhans cells
Degranulation (eosinophils)
FcγRIIB1 (CD32) IgG Low (Kd > 10-7 M) B Cells
Mast cells
No phagocytosis
Inhibition of cell activity
FcγRIIB2 (CD32) IgG Low (Kd > 10-7 M) Macrophages
Inhibition of cell activity
FcγRIIIA (CD16a) IgG Low (Kd > 10-6 M) NK cells Induction of antibody-dependent cell-mediated cytotoxicity (ADCC)
FcγRIIIB (CD16b) IgG Low (Kd > 10-6 M) Eosinophils
Mast cells
Follicular dendritic cells
Induction of microbe killing
FcεRI IgE High (Kd ~ 10-10 M) Mast cells
Langerhans cells
FcεRII (CD23) IgE Low (Kd > 10-7 M) B cells
Langerhans cells
Possible adhesion molecule
FcαRI (CD89) IgA Low (Kd > 10-6 M) Monocytes
Induction of microbe killing
Fcα/μR IgA and IgM High for IgM, Mid for IgA B cells
Mesangial cells
Induction of microbe killing
FcRn IgG Monocytes
Dendritic cells
Epithelial cells
Endothelial cells
Transfers IgG from a mother to fetus through the placenta
Transfers IgG from a mother to infant in milk
Protects IgG from degradation

Functions of Fc receptors

  Fc receptors are found on some cells of the immune system. These include phagocytes like macrophages and monocytes, granulocytes like neutrophils and eosinophils, and lymphocytes of the innate immune system (natural killer cells) or adaptive immune system (e.g. B cells).[14][15][16] They allow these cells to bind to antibodies that are attached to the surface of microbes or microbe infected cells, helping these cells to identify and eliminate microbial pathogens. The Fc receptors bind the antibodies at their Fc region (or tail), an interaction that activates the cell that possesses the Fc receptor.[17] Activation of phagocytes is the most common function attributed to Fc receptors. For example, macrophages begin to ingest and kill an IgG coated pathogen by phagocytosis following engagement of their Fcγ receptors.[18] Another process involving Fc receptors is called antibody-dependent cell-mediated cytotoxicity (ADCC). During ADCC, FcγRIII receptors on the surface of natural killer (NK) cells stimulate the NK cells to release cytotoxic molecules from their granules to kill antibody covered target cells.[19] FcεRI has a different function. FcεRI is the Fc receptor on granulocytes, that is involved in allergic reactions and defense against parasitic infections. When an appropriate allergic antigen or parasite is present, the cross-linking of a least two of IgE molecules and their Fc receptors on the surface of a granulocyte will trigger the cell to rapidly release preformed mediators from its granules.[2]

Signaling mechanisms of Fc receptors

Fc gamma receptors generate signals within their cells through an important activation motif known as an Immunoreceptor tyrosine-based activation motif (ITAM).[20] An ITAM is a specific sequence of amino acids (YXXL) occurring twice in close succession in the intracellular tail of a receptor. When phosphate groups are added to the tyrosine (Y) residue of the ITAM by enzymes called tyrosine kinases, a signaling cascade is generated within the cell. This phosphorylation reaction typically follows interaction of an Fc receptor with its ligand. An ITAM is present in the intracellular tail of FcγRIIA, and its phosphorylation induces phagocytosis in macrophages. FcγRI and FcγRIIIA do not have an ITAM but can transmit an activating signal to their phagocytes by interacting with another protein that does. This adaptor protein is called the Fcγ subunit and, like FcγRIIA, contains the two YXXL sequences that are characteristic of an ITAM. The presence of only one YXXL motif is not sufficient to activate cells, and represents a motif (I/VXXYXXL) known as an Immunoreceptor tyrosine-based inhibitory motif (ITIM). FcγRIIB1 and FcγRIIB2 have an ITIM sequence and are inhibitory Fc receptors; they do not induce phagocytosis. Inhibitory actions of these receptors are controlled by enzymes that remove phosphate groups from tyrosine residues; the phosphatases SHP-1 and SHIP-1 inhibit signaling by Fcγ receptors.[21]

Cellular activation by Fc Receptors


Fc receptors on phagocytes

When IgG molecules, specific for a certain antigen or surface component, bind to the pathogen with their Fab region (fragment antigen binding region), their Fc regions point outwards, in direct reach of phagocytes. Phagocytes bind those Fc regions with their Fc receptors.[18] Many low affinity interactions are formed between receptor and antibody that work together to tightly bind the antibody coated microbe. The low individual affinity prevents Fc receptors from binding antibodies in the absence of antigen, and therefore reduces the chance of immune cell activation in the absence of infection. This also prevents agglutination (clotting) of phagocytes by antibody when there is no antigen. After a pathogen has been bound, interactions between the Fc region of the antibody and the Fc receptors of the phagocyte results in the initiation of phagocytosis. The pathogen becomes engulfed by the phagocyte by an active process involving the binding and releasing of the Fc region/Fc receptor complex, until the cell membrane of the phagocyte completely encloses the pathogen.[22]

Fc receptors on NK cells

The Fc receptor on NK cells recognize IgG that is bound to the surface of a pathogen-infected target cell and is called CD16 or FcγRIII.[23] Activation of FcγRIII by IgG causes the release of cytokines such as IFN-γ that signal to other immune cells, and cytotoxic mediators like perforin and granzyme that enter the target cell and promote cell death by triggering apoptosis. This process is known as antibody-dependent cell-mediated cytotoxicity (ADCC). FcγRIII on NK cells can also associate with monomeric IgG (i.e. IgG that is not antigen-bound). When this occurs, the Fc receptor inhibits the activity of the NK cell.[24]

Fc receptors on mast cells

  IgE antibodies bind to antigens of allergens. These allergen bound IgE molecules interact with Fcε receptors on the surface of mast cells. Activation of mast cells following engagement of FcεRI results in a process called degranulation, whereby the mast cell releases preformed molecules from their cytoplasmic granules; these are a mixture of compounds including histamine, proteoglycans and serine proteases.[25] Activated mast cells also synthesize and secrete lipid-derived mediators (such as prostaglandins, leukotrienes, and platelet-activating factor) and cytokines (such as interleukin 1, interleukin 3, interleukin 4, interleukin 5, interleukin 6, interleukin 13, tumor necrosis factor-alpha, GM-CSF and several chemokines.[26][27] These mediators contribute to inflammation by attracting other leukocytes.

Fc receptors on eosinophils

Large parasites like the helminth (worm) Schistosoma mansoni are too large for ingestion by phagocytes. They also have an external structure called an integument that is resistant to attack by substances released by macrophages and mast cells. However, these parasites can become coated with IgE and recognized by FcεRI on the surface of eosinophils. Activated eosinophils release preformed mediators such as major basic protein, and enzymes such as peroxidase, against which helminths are not resistant.[28][29] The interaction of the FcεRI receptor with the Fc portion of helminth bound IgE causes the eosinophil to release these molecules in a mechanism similar to that of the NK cell during ADCC.[30]

See also

  • Fc receptor-like molecule

Further reading

  • Immunobiology. 5th ed. Janeway, Charles A.; Travers, Paul; Walport, Mark; Shlomchik, Mark. New York and London: Garland Publishing; c2001.
  • Cellular and molecular immunology / Abul K. Abbas, Andrew H. Lichtman ; illustrations by David L. Baker, Alexandra Baker. Philadelphia, PA : Elsevier Saunders, c2005
  • Stimulatory and inhibitory signals originating from the macrophage Fcγ receptors. Jeffrey S. Gerber and David M. Mosser. Microbes Infect. 2001 Feb;3(2):131-9.


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This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Fc_receptor". A list of authors is available in Wikipedia.
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